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Clinical Research Nurse (Ad-Hoc) - Boston
Job Description
Position: Mobile Research Nurse
Job Description: As a Mobile Research Nurse, you will play a crucial role in ensuring the successful execution of research studies. You will be responsible for administering investigational medications/products, conducting patient assessments, collecting vital information, and adhering to study protocols with utmost accuracy and ethics. Your expertise and caring nature will help us maintain compliance with each study's protocol and safeguard the well-being of study patients. Principal Duties and Responsibilities:
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- Accountable for the competent and confident delivery of high-quality clinical care to patients/participants. Ensure compliance with each study’s protocol by providing thorough review and documentation at each subject study visit.
- Administer investigational medications/products as needed; Perform patient assessments to determine presence of side effects; notify Principal Investigator of findings/issues.
- Perform medical tests as outlined in protocol, including, but not limited to: vital signs, specimen collection, electrocardiograms; Process specimens and ship specimens per protocol.
- Provide patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment.
- Responsible for adherence to clinical research policies to ensure ethical conduct and protect vulnerable populations.
- Communicate effectively, promoting open and trusting relationships.
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- Relevant Nurse Licensure
- CH-GCP Certificate
- Graduate from an accredited BSN or Associate Degree in Nursing or Nursing Diploma
- program
- Minimum 2 years’ post qualification acute care experience
- Clinical Research experience desirable
- BLS certification required
- Experience and knowledge of working in clinical research trials with ICH-GCP (Good
- Clinical Practice) Certification - (Training can be provided)
- Good basic IT skills, utilizing mobile devices and Microsoft systems
- Trained in Handling and Transport of Hazardous Substances (training can be provided)
- A flexible schedule is essential
- Unencumbered driver’s license, reliable car
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- Competitive pay rates with hourly compensation for travel time and patient interactions.
- Mileage reimbursement for travel expenses.
- Flexible working shifts to accommodate work-life balance.
- Project-specific training provided to enhance your skills in clinical research.
- Ongoing training and line management support for professional growth.
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
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